Transcript #00024067 (NM_144499.2, GNAT1 gene)

Transcript name transcript variant 1
Gene name GNAT1 (guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1)
Chromosome 3
Transcript - NCBI ID NM_144499.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_653082.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2015-10-24 15:30:34 +02:00 (CEST)
Date last edited N/A


Variants

81 entries on 1 page. Showing entries 1 - 81.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-3679C>T r.(?) p.(=)
?/. - c.-3652A>G r.(?) p.(=)
+/. - c.8del r.(?) p.(Ala3Valfs*17)
-?/. - c.15C>T r.(?) p.(Ala5=)
-?/. - c.39G>A r.(?) p.(Arg13=)
-?/. - c.39G>A r.(?) p.(Arg13=)
+?/. - c.51del r.(?) p.(Lys18Serfs*2)
-?/. - c.66C>T r.(?) p.(Asp22=)
+?/. 1 c.98T>C r.(?) p.(Leu33Pro)
?/. - c.107G>A r.(?) p.(Gly36Asp)
+/. - c.113G>A r.(?) p.(Gly38Asp)
+/. - c.113G>A r.(?) p.(Gly38Asp)
+/. - c.113G>A r.(?) p.(Gly38Asp)
+/. - c.113G>A r.(?) p.(Gly38Asp)
+/. - c.113G>A r.(?) p.(Gly38Asp)
+/. - c.113G>A r.(?) p.(Gly38Asp)
?/. 2 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. 6 c.113G>A r.(?) p.(Gly38Asp)
+?/. - c.124A>G r.(?) p.(Lys42Glu)
-/. - c.150-17G>A r.(=) p.(=)
+?/. 3 c.155T>A r.(?) p.(Ile52Asn)
+?/. 3 c.155T>A r.(?) p.(Ile52Asn)
+?/. 3 c.218C>T r.(?) p.(Thr73Met)
+?/. - c.218C>T r.(?) p.(Thr73Met)
+/. 3 c.282del r.(?) p.(Ala95Hisfs*9)
+/. - c.282del r.(?) p.(Ala95Hisfs*9)
?/. - c.291G>C r.(?) p.(Gln97His)
-?/. - c.292-3C>T r.spl? p.?
-/. - c.294C>T r.(?) p.(Asp98=)
-?/. - c.294C>T r.(?) p.(Asp98=)
+/. 4 c.359C>A r.(?) p.(Ser120*)
?/. - c.379T>C r.(?) p.(Trp127Arg)
?/. - c.379T>C r.(?) p.(Trp127Arg)
+/. 4 c.386A>G r.(?) p.(Asp129Gly)
+/. 4 c.386A>G r.(?) p.(Asp129Gly)
+?/. - c.413G>A r.(?) p.(Arg138His)
-/. - c.449+34_449+40dup r.(=) p.(=)
+?/. - c.460G>T r.(?) p.(Asp154Tyr)
+?/. 5 c.508G>A r.(?) p.(Val170Met)
+?/. - c.508G>A r.(?) p.(Val170Met)
?/. - c.514C>G r.(?) p.(Arg172Gly)
?/. - c.574T>C r.(?) p.(Phe192Leu)
?/. - c.586G>A r.(?) p.(Asp196Asn)
?/. - c.595G>A r.(?) p.(Gly199Arg)
+/. - c.598C>G r.(?) p.(Gln200Glu)
-?/. - c.633C>T r.(?) p.(Phe211=)
?/. - c.653T>C r.(?) p.(Ile218Thr)
?/. - c.653T>C r.(?) p.(Ile218Thr)
+?/. 6 c.653T>C r.(?) p.(Ile218Thr)
+?/. - c.653T>C r.(?) p.(Ile218Thr)
-?/. - c.708+10A>T r.(=) p.(=)
?/. - c.734T>A r.(?) p.(Leu245Gln)
+/. - c.753C>A r.(?) p.(Asn251Lys)
?/. - c.782T>A r.(?) p.(Val261Glu)
+?/. - c.803A>C r.(?) p.(Asp268Ala)
?/. - c.805G>C r.(?) p.(Val269Leu)
+?/. 7 c.818_820del r.(?) p.(Lys273del)
+?/. 7 c.818_820del r.(?) p.(Lys273del)
+?/. 7 c.818_820del r.(?) p.(Lys273del)
+?/. - c.819G>T r.(?) p.(Lys273Asn)
+/. - c.863-2A>G r.spl p.(?)
+/. - c.863-2A>G r.spl p.?
-?/. - c.876C>T r.(?) p.(Tyr292=)
-/. - c.876C>T r.(?) p.(Tyr292=)
+/. - c.904C>T r.(?) p.(Gln302*)
+?/. - c.904C>T r.(?) p.(Gln302Ter)
+?/. 8 c.963C>A r.(?) p.(Cys321*)
?/. - c.986A>C r.(?) p.(Lys329Thr)
?/. - c.1041dup r.(?) p.(Gly348Trpfs*86)
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